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. 2004 May;57(5):563–568. doi: 10.1111/j.1365-2125.2004.02059.x

Table 2.

Presents the pharmacokinetics of levofloxacin for plasma (n = 7), inflamed and healthy subcutaneous adipose tissue (n = 6). Data are shown as mean ± SD and (95% confidence intervals)

Compartment AUC(0,10 h) tissue : AUC(0,10 h) free plasma ratio AUC(0,10 h) (mg l−1 h) AUC(0,24 h) (mg l−1 h) plasma Cmax (mg l−1) tmax (h) t½β (h) CL (l h−1 kg−1) Vz (l kg−1)
Plasma, total 32.3 ± 7.3 52.1 ± 17.3 8.37 ± 1.93 0.52 ± 0.26 10.0 ± 6.3 0.12 ± 0.05 1.35 ± 0.30
  (n = 7) (25.5–39.1) (36.0–68.1) (6.6–10.2) (0.28–0.77) (4.2–16.0) (0.07–0.16) (1.08–1.63)
Tissue Inflamed 1.15 ± 0.95 25.5 ± 16.8 5.45 ± 3.74 1.06 ± 0.14
  (n = 6) (0.15–2.15) (7.9–43.1) n.d. (1.53–9.37) (0.91–1.20) n.d. n.d. n.d.
Tissue Healthy 1.06 ± 0.61 23.5 ± 10.0 4.42 ± 2.09 1.39 ± 1.29
  (n = 6) (0.43–1.70) (13.0–33.9) n.d. (2.22–6.61) (0.04–2.74) n.d. n.d. n.d.

n.d: not determined.